66949-138 / 3285 Hand San Foam

Zep Foaming Hand Sanitizer by

Drug Labeling and Warnings

Zep Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Zep Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ZEP FOAMING HAND SANITIZER- ethanol liquid 
Zep Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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66949-138 / 3285 Hand San Foam

Active ingredient

Ethanol 70% v/v

Purpose

Antiseptic

Uses

• To help reduce germs and bacteria on the skin.
• Recommended for repeated use.
• No rinsing required.

Warnings

Flammable. Keep away from fire, flame or spark.

For external use only.
Do not use in the eye; if in eyes, rinse thoroughly with water.

When using this product

• Do not swallow.
• If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to drink and consult a physician immediately.

Stop use and ask a doctor

Stop use and ask a doctor if skin irritation or redness persists for more than 72 hours.

Keep out of reach of children and pets

Keep out of reach of children and pets. Children must be supervised in use of this product.

Directions

• Apply foam to hands.
• Rub into hands for at least 20 seconds or until dry.

Other information

• Keep container closed and stored in a dry area at temperatures between 68°F to 77°F (20°C and 25°C).
• Do not reuse empty container.
• Dispose in accordance with all applicable federal, state and local regulations.

Inactive ingredients

Aqua, Acrylates/Perfluorohexylethyl Methacrylate Copolymer (and) Perfluorohexylethyl Alcohol, Aloe Barbadensis Leaf Juice

Questions or comments?

Call 1-877-I-BUY-ZEP (1-877-428-9937)

ZEP FOAMING HAND SANITIZER 
ethanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-138
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
2-(PERFLUOROHEXYL)ETHANOL (UNII: G2R5YO5N3V)
BUTYL ACRYLATE/METHYL METHACRYLATE/PERFLUOROHEXYLETHYL METHACRYLATE COPOLYMER (SALUS AF) (UNII: HLB263IJK9)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-138-24	15140 mL in 1 CASE; Type 0: Not a Combination Product	09/01/2021	12/31/2022
2	NDC: 66949-138-16	4800 mL in 1 CASE; Type 0: Not a Combination Product	09/01/2021	12/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/01/2021	12/31/2022

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		112125310	manufacture(66949-138)

Revised: 1/2023

Document Id: f1ed7811-cdcc-23f4-e053-2a95a90af36b

34390-5

Set id: c72cf71f-e63a-2854-e053-2a95a90ab30e

Version: 3

Effective Time: 20230110